HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20264Generated: October 29, 2026
Butyl iodide → HCID 86598518, compound
https://huagongshe.com/reaction/20264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 13523271 | HCID 13523271 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86598518 | HCID 86598518 | 69% |
Reaction Steps
To a solution of (2R,4S)-2-tert-butyl-3-formyloxazolidine-4-carboxylic acid methyl ester (4.6 g, 21.4 mmol) [see D. Seebach, J. D. Aebi, M. Gander-Coquoz and R. Naef, Helv. Chim. Acta., 70, 1194 (1987)] in dry THF (120 mL) under N2 was added 1-iodobutane (12.2 mL, 106.8 mmol) and HMPA (12 mL). The mixture was cooled to −78° C. and a solution of sodium bis(trimethylsilyl)amide in THF (1 M, 32 mL, 32 mmol) was added dropwise over 15 minutes. After 2 h, the reaction mixture was warmed to 0° C. and quenched with saturated aqueous NH4Cl (200 mL). The quenched reaction mixture was diluted with ether (400 mL) and washed with water (3×200 mL) and brine (200 mL), then dried (Na2SO4) and filtered. Concentration of the filtrate and flash chromatography of the residue (20% ethyl acetate/hexanes) provided the title compound as a pale brown solid (4.0 g, 69%). MS(ES) m/e 272 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07745637B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-50d8dfd3760f45d5ae82826e18b0a2f3 |
|---|
| Source note | uspto-grants-2010_06 |
|---|